1. Halama, Niels, Grauling-Halama, Silke A, Jäger, Dirk. . Identification and characterization of the human StARD9 gene in the LGMD2A-region on chromosome 15q15 by in silico methods. In International journal of molecular medicine, 18, 653-6. doi:. https://pubmed.ncbi.nlm.nih.gov/16964419/
2. Okamoto, Nobuhiko, Tsuchiya, Yuki, Miya, Fuyuki, Kosaki, Kenjiro, Kitagawa, Daiju. 2017. A novel genetic syndrome with STARD9 mutation and abnormal spindle morphology. In American journal of medical genetics. Part A, 173, 2690-2696. doi:10.1002/ajmg.a.38391. https://pubmed.ncbi.nlm.nih.gov/28777490/
3. Chen, Xiaowei Sylvia, Reader, Rose H, Hoischen, Alexander, Newbury, Dianne F, Fisher, Simon E. 2017. Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment. In Scientific reports, 7, 46105. doi:10.1038/srep46105. https://pubmed.ncbi.nlm.nih.gov/28440294/
4. Karoii, Danial Hashemi, Azizi, Hossein, Skutella, Thomas. 2024. Whole transcriptome analysis to identify non-coding RNA regulators and hub genes in sperm of non-obstructive azoospermia by microarray, single-cell RNA sequencing, weighted gene co-expression network analysis, and mRNA-miRNA-lncRNA interaction analysis. In BMC genomics, 25, 583. doi:10.1186/s12864-024-10506-9. https://pubmed.ncbi.nlm.nih.gov/38858625/
5. Cheng, Tao, Shuang, Weibing, Ye, Dawen, Xu, Weiqiang, Guan, Chao. 2021. SNHG16 promotes cell proliferation and inhibits cell apoptosis via regulation of the miR-1303-p/STARD9 axis in clear cell renal cell carcinoma. In Cellular signalling, 84, 110013. doi:10.1016/j.cellsig.2021.110013. https://pubmed.ncbi.nlm.nih.gov/33901578/
6. Sun, Yanfa, Wu, Qiong, Lin, Rulong, Jiang, Xiaobing, Li, Yan. 2023. Genome-wide association study for the primary feather color trait in a native Chinese duck. In Frontiers in genetics, 14, 1065033. doi:10.3389/fgene.2023.1065033. https://pubmed.ncbi.nlm.nih.gov/36936414/
7. Liang, Shanhui, Ge, Huijuan, Zhou, Shuling, Wu, Xiaohua, Li, Jin. 2024. Prognostic factors of 87 ovarian yolk sac tumor (OYST) patients and molecular characteristics of persistent and recurrent OYST. In Gynecologic oncology, 187, 64-73. doi:10.1016/j.ygyno.2024.05.001. https://pubmed.ncbi.nlm.nih.gov/38733954/
8. Smith, Tara C, Fang, Zhiyou, Luna, Elizabeth J. . Novel interactors and a role for supervillin in early cytokinesis. In Cytoskeleton (Hoboken, N.J.), 67, 346-64. doi:10.1002/cm.20449. https://pubmed.ncbi.nlm.nih.gov/20309963/
9. Lin, Li-Han, Chang, Kuo-Wei, Cheng, Hui-Wen, Liu, Chung-Ji. 2023. Identification of Somatic Mutations in Plasma Cell-Free DNA from Patients with Metastatic Oral Squamous Cell Carcinoma. In International journal of molecular sciences, 24, . doi:10.3390/ijms241210408. https://pubmed.ncbi.nlm.nih.gov/37373553/
10. Çolak-Geniş, Esra, Özdemir Erdoğan, Müjdan, Çam, Fethi Sırrı, Gerik-Celebi, Hamide Betül, Solak, Mustafa. 2024. Investigation of Genetic Changes in Three Families with Bipolar Disease. In Molecular syndromology, 15, 464-473. doi:10.1159/000539115. https://pubmed.ncbi.nlm.nih.gov/39634238/
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